HGVS | Genome Assembly |
---|---|
NC_000016.10:g.67436767G>A , CM000678.2:g.67436767G>A | GRCh38 |
NC_000016.9:g.67470670G>A , CM000678.1:g.67470670G>A | GRCh37 |
NC_000016.8:g.66028171G>A | NCBI36 |
NG_011482.1:g.49420C>T | |
NG_016549.1:g.10635G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326152.6:c.982G>A MANE Select | ENSP00000316786.5:p.Ala328Thr | |
ENST00000326152.5:c.982G>A | ENSP00000316786.5:p.Ala328Thr | |
NM_000196.3:c.982G>A | NP_000187.3:p.Ala328Thr | |
NM_000196.4:c.982G>A MANE Select | NP_000187.3:p.Ala328Thr |